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United States Patent |
5,631,195
|
Yanagisawa
,   et al.
|
May 20, 1997
|
Glass composition and substrate for plasma display
Abstract
A glass composition comprising from 45 to 66 wt % of SiO.sub.2, from 0 to
15 wt % of Al.sub.2 O.sub.3, from 10 to 24 wt % of Li.sub.2 O+Na.sub.2
O+K.sub.2 O, from 14 to 26 wt % of CaO+MgO+SrO+BaO+ZnO, and from 0 to 1 wt
% of SO.sub.3 +Sb.sub.2 O.sub.3, said glass composition containing
substantially no zirconia and having a strain point of at least
560.degree. C. and a linear thermal expansion coefficient of at least
80.times.10.sup.-7 /.degree.C. within a temperature range of from
50.degree. to 350.degree. C.
Inventors:
|
Yanagisawa; Osamu (Yokohama, JP);
Oda; Kenji (Yokohama, JP);
Sugimoto; Naoki (Yokohama, JP);
Takegawa; Yoshio (Kawasaki, JP);
Takada; Akira (Yokohama, JP);
Osada; Hideyo (Yokohama, JP);
Aizawa; Haruo (Yokohama, JP);
Miura; Koji (Yokohama, JP)
|
Assignee:
|
Asahi Glass Company Ltd. (Tokyo, JP)
|
Appl. No.:
|
528265 |
Filed:
|
September 14, 1995 |
Foreign Application Priority Data
Current U.S. Class: |
501/72; 501/69; 501/70 |
Intern'l Class: |
C03C 003/078; C03C 003/085; C03C 003/087 |
Field of Search: |
501/69,70,72
|
References Cited
U.S. Patent Documents
3464932 | Sep., 1969 | Connelly et al. | 501/69.
|
3808154 | Apr., 1974 | Omori | 501/70.
|
3819972 | Jun., 1974 | Sanner | 501/69.
|
4015966 | Apr., 1977 | Weaver | 501/69.
|
4994415 | Feb., 1991 | Imai et al. | 501/66.
|
5116788 | May., 1992 | Dumbaugh, Jr. | 501/66.
|
5116789 | May., 1992 | Dumbaugh, Jr. et al. | 501/66.
|
5326730 | Jul., 1994 | Dumbaugh, Jr. et al. | 501/69.
|
5374595 | Dec., 1994 | Dumbaugh, Jr. et al. | 501/66.
|
5459109 | Oct., 1995 | Lapp | 501/66.
|
Foreign Patent Documents |
3-40933 | Feb., 1991 | JP.
| |
9611887 | Apr., 1996 | WO.
| |
Primary Examiner: Bell; Mark L.
Assistant Examiner: Troilo; Louis M.
Attorney, Agent or Firm: Oblon, Spivak, McClelland, Maier & Neustadt, P.C.
Claims
What is claimed is:
1. A glass composition comprising from 50 to 66 wt % of SiO.sub.2, from 0
to 15 wt % of Al.sub.2 O.sub.3, from 0 to 13.4 wt % of K.sub.2 O, from 10
to 24 wt % of Li.sub.2 O+Na.sub.2 O+K.sub.2 O, from 0 to 7 wt % of BaO,
from 14 to 26 wt % of CaO+MgO+SrO+BaO+ZnO, and from 0 to 1 wt % of
SO.sub.3 +Sb.sub.2 O.sub.3, said glass composition containing
substantially no zirconia and having a strain point of at least
560.degree. C. and a linear thermal expansion coefficient of at least
80.times.10.sup.7 /.degree.C. within a temperature range of from
50.degree. to 350.degree. C.
2. The glass composition according to claim 1, which has a linear thermal
expansion coefficient of from 80.times.10.sup.-7 to 120.times.10.sup.-7
/.degree.C. within a temperature range of from 50.degree. to 350.degree.
C.
3. The glass composition according to claim 1, which has a linear thermal
expansion coefficient of from 80.times.10.sup.-7 to 95.times.10.sup.-7
/.degree.C. within a temperature range of from 50.degree. to 350.degree.
C.
4. The glass composition according to claim 1, wherein the liquidus
temperature is lower than the temperature at which the viscosity is
10.sup.4 poise.
5. The glass composition according to claim 1, which contains substantially
no arsenic.
6. The glass composition according to claim 1, which comprises from 50 to
63 wt % of SiO.sub.2, from 5.5 to 15 wt % of Al.sub.2 O.sub.3, from 0 to 6
wt % of Na.sub.2 O, from 1 to 13.4 wt % of K.sub.2 O, from 0 to 0.5 wt %
of Li.sub.2 O, from 10 to 24 wt % of Li.sub.2 O+Na.sub.2 O+K.sub.2 O, from
0 to 14 wt % of CaO, from 0 to 6 wt % of MgO, from 1 to 14 wt % of SrO,
from 0 to 7 wt % of BaO, from 0 to 6 wt % of ZnO, from 14 to 26 wt % of
CaO+MgO+SrO+BaO+ZnO, and from 0 to 1 wt % of SO.sub.3 +Sb.sub.2 O.sub.3,
and which contains substantially no zirconia.
7. The glass composition according to claim 6, which has a strain point of
at least 570.degree. C.
8. A substrate for plasma display which is made of a glass composition
comprising from 50 to 66 wt % of SiO.sub.2, from 0 to 15 wt % of Al.sub.2
O.sub.3, from 0 to 13.4 wt % K.sub.2 O, from 10 to 24 wt % Li.sub.2
O+Na.sub.2 O+K.sub.2 O, from 0 to 7 wt % of BaO, from 14 to 26 wt % of
CaO+MgO+SrO+BaO+ZnO, and from 0 to 1 wt % of SO.sub.3 +Sb.sub.2 O.sub.3,
said glass composition containing substantially no zirconia and having a
strain point of at least 560.degree. C. and a linear thermal expansion
coefficient of at least 80.times.10.sup.-7 /.degree.C. within a
temperature range of from 50.degree. to 350.degree. C.
9. A substrate for plasma display which is made of a glass composition
comprising from 50 to 63 wt % of SiO.sub.2, from 5.5 to 15 wt % of
Al.sub.2 O.sub.3, from 0 to 6 wt % of Na.sub.2 O, from 1 to 13.4 wt %
K.sub.2 O, from 0 to 0.5 wt % Li.sub.2 O, from 10 to 24 wt % Li.sub.2
O+Na.sub.2 O+K.sub.2 O, from 0 to 14 wt % of CaO, from 0 to 6 wt % of MgO,
from 1 to 14 wt % of SrO, from 0 to 7 wt % of BaO, from 0 to 6 wt % of
ZnO, from 14 to 26 wt % of CaO+MgO+SrO+BaO+ZnO, and from 0 to 1 wt % of
SO.sub.3 +Sb.sub.2 O.sub.3 and which contains substantially no zirconia.
Description
BACKGROUND OF THE INVENTION
FIELD OF THE INVENTION
The present invention relates to a glass composition suitable for
substrates for display devices such as fluorescent character display
tubes, plasma display panels, flat cathode ray tubes and liquid crystal
display tubes.
As a glass substrate for plasma display, a soda lime glass having a strain
point of about 510.degree. C., formed by float process, is commonly used.
A typical plasma display panel is produced by the following process.
Firstly, on a glass substrate for the display surface side, display
electrodes will be printed, and dielectric layer will be printed thereon,
followed by baking. Further, a protective film will be vapor-deposited on
this dielectric layer. On the other hand, on the opposing rear-side glass
substrate, Al, Ag or Ni electrodes, and stripe-shaped partition walls (low
melting point glass) to prevent electric discharge between electrodes and
to prevent color mixing of red-, green- and blue-phosphors, will be formed
by baking at a temperature of from 500.degree. to 600.degree. C. Further,
printed circuits will be formed, and red-, green- and blue-phosphors will
be printed.
The display side and rear side glass substrates will be bonded by means of
a low melting temperature glass frit within the same temperature range as
the above-mentioned temperature, and a gas mixture of xenon and neon as
the main discharge gas, will be sealed in to obtain a plasma display
panel.
The glass substrate for plasma display is subjected to heat treatment at a
temperature equal to or higher than the strain point of soda lime glass at
a level of from 500.degree. to 600.degree. C., and thermal deformation is
likely to take place. Therefore, when soda lime glass substrates are used,
a 40 inch panel is almost at the limit, and it is substantially difficult
to use soda lime glass substrates for high definition TV which requires a
panel of a larger size with a high level of resolution.
A ZrO.sub.2 -containing glass is also known which undergoes a less degree
of deformation by such heat treatment (Japanese Unexamined Patent
Publication No. 40933/1991). However, this glass is susceptible to
scratching, and it is necessary not to polish the glass or to polish with
a due care not to form a substantial scratch mark. Further, even with a
glass having no scratch mark, a scratch mark may form during the
production process. Therefore, a due care will be required for handling in
the process.
Each of these methods reduces the amount of glass substrate which can be
produced per unit period of time. In other words, each method has a
problem that the production cost of glass increases.
SUMMARY OF THE INVENTION
It is an object of the present invention to provide a glass composition
which scarcely undergoes thermal deformation and which is hardly
susceptible to scratching.
That is, the present invention provides a glass composition comprising from
45 to 66 wt % of SiO.sub.2, from 0 to 15 wt % of Al.sub.2 O.sub.3, from 10
to 24 wt % of Li.sub.2 O+Na.sub.2 O+K.sub.2 O, from 14 to 26 wt % of
CaO+MgO+SrO+BaO+ZnO, and from 0 to 1 wt % of SO.sub.3 +Sb.sub.2 O.sub.3,
said glass composition containing substantially no zirconia and having a
strain point of at least 560.degree. C. and a linear thermal expansion
coefficient of at least 80.times.10.sup.-7 /.degree.C. within a
temperature range of from 50.degree. to 350.degree. C.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Now, the reason for the definition of the composition of the glass
composition of the present invention will be described.
In the present invention, if the glass composition contains ZrO.sub.2
substantially, the glass tends to be susceptible to scratching, and the
breakage frequency during the production process tends to be high, whereby
the production yield will be poor. Therefore, the glass composition of the
present invention contains substantially no zirconia. Here, "contains
substantially no zirconia" means that the zirconia content is less than
0.2 wt %.
Further, if the glass composition contains As.sub.2 O.sub.3 substantially,
arsenic will dissolve in the polishing waste liquid resulting from
polishing in the commercial production, whereby a substantial cost will be
required for treatment of the waste liquid. Therefore, the glass
composition preferably contains substantially no arsenic. Here, "contains
substantially no arsenic" means that the As.sub.2 O.sub.3 content is less
than 0.1 wt %.
Further, if the glass composition contains B.sub.2 O.sub.3 substantially,
the linear expansion coefficient tends to be small, and boron tends to
evaporate during the production process, whereby it tends to be difficult
to produce a uniform glass. Further, evaporated boron is likely to erode
the bricks of the furnace. Accordingly, it is preferred that the
composition does not substantially contain B.sub.2 O.sub.3. Here, "does
not substantially contain B.sub.2 O.sub.3 " means that the content is less
than 0.1 wt %.
If the linear thermal expansion coefficient is less than 80.times.10.sup.-7
/.degree.C., within a temperature range of from 50.degree. to 350.degree.
C., cracks are likely to form in the electrodes and the partition walls.
Therefore, the linear thermal expansion coefficient is at least
80.times.10.sup.-7 /.degree.C., preferably at least 85.times.10.sup.-7
/.degree.C. Further, the linear thermal expansion coefficient is
preferably less than 120.times.10.sup.-7 /.degree.C., more preferably less
than 95.times.10.sup.-7 /.degree.C.
If the strain point is less than 560.degree. C., thermal deformation is
likely to form during the heat treatment of e.g. electrodes and partition
walls. Therefore, the strain point is usually at least 560.degree. C.,
preferably at least 570.degree. C.
SiO.sub.2 is a main component for the glass. If the content of SiO.sub.2 is
less than 45 wt %, the chemical durability tends to be poor, particularly
corrosion by hydrofluoric acid tends to be substantial. On the other hand,
if it exceeds 66 wt %, the linear thermal expansion coefficient will be
less than 80.times..sup.-7 /.degree.C. Therefore, the SiO.sub.2 content is
from 45 to 66 wt %. It is preferably within a range of from 50 to 63 wt %
in order to obtain a higher strain point (at least 570.degree. C.).
Al.sub.2 O.sub.3 which may optionally be used, is a component which is
effective to increase the strain point without substantially reducing the
linear thermal expansion coefficient. If the content of Al.sub.2 O.sub.3
exceeds 15 wt %, the liquidus temperature tends to be too high. Therefore,
the content of Al.sub.2 O.sub.3 is usually within a range of from 0 to 15
wt %, preferably from 0.5 to 12 wt %, more preferably from 5.5 to 10 wt %.
Li.sub.2 O, Na.sub.2 O and K.sub.2 O are components which are effective for
adjusting the linear thermal expansion coefficient of glass or the
viscosity at a high temperature. These components may not all be
incorporated simultaneously. However, if their total content is less than
10 wt %, the linear thermal expansion coefficient tends to be less than
80.times.10.sup.-7 /.degree.C., and if it exceeds 24 wt %, it becomes
difficult to bring the strain point to a level of at least 560.degree. C.
Therefore, their total content is within a range of from 10 to 24 wt %.
The content of Na.sub.2 O is preferably from 0 to 6 wt %, and the content
of K.sub.2 O is preferably from 0 to 0.5 wt %.
Among them, K.sub.2 O has an effect of increasing the strain point, and its
content is preferably from 4 to 20 wt %, particularly from 9 to 16 wt %.
SrO, BaO, ZnO, CaO and MgO may not all be incorporated simultaneously.
However, if their total content is less than 14 wt %, it tends to be
difficult to bring the strain point to a level of at least 560.degree. C.
On the other hand, if it exceeds 26 wt %, the strain point tends to be too
low. Therefore, their total content is usually within a range of from 14
to 26 wt %, preferably from 17 to 23 wt %, more preferably from 18 to 20
wt %.
The content of CaO is preferably from 0 to 14 wt %, the content of MgO is
preferably from 0 to 6 wt %, the content of BaO is preferably from 0 to 14
wt %, and the content of ZnO is preferably from 0 to 6 wt %.
Among them, SrO has an effect of increasing the strain point, and its
content is preferably from 1 to 14 wt %, particularly from 4 to 10 wt %.
Further, CaO is preferably contained in an amount of from 1 to 14 wt %.
Sb.sub.2 O.sub.3 and SO.sub.3 which may optionally be incorporated, are
refining agents. If their total content exceeds 1 wt %, their effects of
refining will be saturated. Therefore, their total content is within a
range of from 0 to 1 wt %.
In addition to the above components, the following components may be
incorporated.
CeO.sub.2 may be incorporated for the purpose of suppressing browning which
is likely to result when the glass is irradiated with X-rays. TiO.sub.2
and Bi.sub.2 O.sub.3 may be incorporated for the purpose of suppressing
solarization which is likely to result when the glass is irradiated with
ultraviolet rays. PbO has an effect of suppressing solarization, but even
if it is added excessively, the effect will be saturated. Therefore, the
content is preferably less than 0.3 wt %, more preferably less than 0.1 wt
%. Further, the color of glass can be controlled by incorporating a small
amount of Fe.sub.2 O.sub.3, CoO, Cr.sub.2 O.sub.3 or NiO.
On the other hand, it is preferred that fluorine, zirconium, boron,
phosphorus and arsenic are not substantially contained, although they may
be incorporated as impurities.
The glass composition of the present invention can be produced by supplying
glass batch formulated to have the desired composition, into a melting
furnace, followed by vitrification and forming into a transparent and not
substantially crystallized sheet glass having a predetermined thickness by
float process.
Now, the present invention will be described in further detail with
reference to Examples. However, it should be understood that the present
invention is by no means restricted by such specific Examples.
EXAMPLES 1 to 6 and COMPARATIVE EXAMPLES 7 to 9
550 g of glass batch formulated to have the desired composition, were put
into a platinum crucible and heated for 4.5 hours for vitrification in a
furnace of 1510.degree. C. while stirring from time to time. Then, the
molten glass was cast in a graphite mold and then annealed to reduce
strain. Table 1 shows the composition by weight % of oxides. The amounts
of CoO and NiO were so small that they were represented by ppm.
With respect to such a sheet glass, the linear thermal expansion
coefficient, the strain point, the brittleness, the temperature at
10.sup.2 poise, which is an index for the solubility, the temperature at
10.sup.4 poise, which is an index for formability, the liquidus
temperature, the chemical durability and the electrical resistance were
measured, and the results are shown in the respective columns in Table 1.
Table 1 also shows Comparative Examples.
Various properties were measured as follows.
The brittleness was determined in such a manner that a Vickers indentator
was pressed against a mirror-polished glass surface under a load of 500 g,
whereupon the diagonal length (a) of the indentation and the crack length
(C) were measured, and their ratio C/a was obtained. The larger the ratio
C/a, the higher the brittleness [Sehgal et al. J. Mat. Sci. letters [14],
p.167-169, 1995].
The chemical durability was represented by the weight reduction per unit
area (mg/cm.sup.2) when a test sample of 50 mm.times.50 mm.times.3 mmt was
immersed in a 15 wt % HF aqueous solution at 40.degree. C. for 90 seconds.
The linear thermal expansion coefficient is represented by a value within a
temperature range of from 50.degree. to 350.degree. C., and the electrical
resistance is represented by a logarithmic value of the resistance (unit:
.OMEGA..multidot.cm) at 150.degree. C. Other physical properties were
measured in accordance with methods which are commonly employed in the
glass industry.
The liquidus temperatures of all glasses in Examples and Comparative
Examples in Table 1, are all lower than the temperatures of the respective
glasses at 10.sup.4 poise. This indicates that they can be formed by float
process. The ratio C/a of the soda lime glass in Comparative Example 9 is
lower than C/a of the glasses in Examples 1 to 8, which indicates that the
strain point is low as compared with that of the glasses in the Examples,
and such soda lime glass can not be used for a plasma display substrate of
a large size with high resolution, although it is scarcely brittle. The
glass in Comparative Example 10 is equivalent to the glasses in Examples 1
to 8 with respect to both the strain point and the linear expansion
coefficient, and the ratio C/a is also small, which indicates that the
glass is scarcely brittle. However, the temperature at 10.sup.2 poise is
higher by as much as 200.degree. C. than those of the glasses of Examples
1 to 8, which indicates that melting is very difficult. The ratio C/a of
the glass in Comparative Example 11 which contains zirconia, is higher
than the ratios C/a of the glasses in Examples 1 to 8, which indicates
that it is readily brittle.
As shown by the foregoing Examples, the glass composition of the present
invention has a high linear thermal expansion coefficient and a high
strain point, and it can relatively easily be melted and scarcely brittle.
TABLE 1
__________________________________________________________________________
Comparative
Examples Examples
Composition 1 2 3 4 5 6 7 8 9 10 11
__________________________________________________________________________
SiO.sub.2 64.4
57.2
61.2
62.4
53.8
62.6
46 64.1
72.3
62.4
57.5
Al.sub.2 O.sub.3
1 5.6 5.7 6.1 5.6 6.1 15 4.2 2 17.1
7
Li.sub.2 O 0 0 0 0 0 0.2 0 0.2 0 0 0
Na.sub.2 O 0 0 0 0 1.0 0 3.2 1.4 12.5
12.2
0
K.sub.2 O 11 10.6
13.4
11.6
9.4 11.6
19.1
10 1 3.8 4.3
SrO 13 5 5.8 9.2 4.3 9.2 6.7 0 0 0 6
BaO 0.4 12.8
0 0 11.4
0 0 7 0 0 9
ZnO 5 0 2.7 0.3 10.2
0.3 0 0 0 0 4
CaO 0 3.4 8.1 10 1.4 10.0
3.6 7.7 8 0.5 0
MgO 5 5 2.8 0 2.9 0 5 5 4 3.5 7
ZrO.sub.2 0 0 0 0 0 0 0 0 0 0 2
CeO.sub.2 0.5 0 0 0 0 0 0 0 0 0 3
TiO.sub.2 0.4 0 0.1 0 0 0 0 0 0 0 0
PbO 0 0.2 0 0 0 0 0 0 0 0 0
Bi.sub.2 O.sub.3
0 0 0 0 0 0 0.3 0 0 0 0
Fe.sub.2 O.sub.3
0 0 0 0 0 0 0.2 0.1 0 0 0
CoO (ppm) 18 0 0 0 0 0 0 0 0 0 0
NiO (ppm) 140 0 0 0 0 0 0 0 0 0 0
SO.sub.3 0.1 0.2 0.2 0 0 0 0.4 0 0.2 0 0
Sb.sub.2 O.sub.3
0.2 0 0 0.4 0 0 0.5 0.3 0 0.5 0.2
Linear expansion
82 85 85 82 83 83 116 82 85 88 82
coefficient (.times. 10.sup.-7 /.degree.C.)
Strain point (.degree.C.)
567 587 587 594 571 586 570 572 511 576 589
Brittleness 2.61
2.97
2.62
2.64
2.91
2.65
3.07
2.63
2.43
2.43
3.16
Temp. at 10.sup.2 poise
1565
1560
1560
1565
1549
1550
1518
1564
1470
1770
1504
Temp. at 10.sup.4 poise
1145
1161
1161
1155
1169
1143
1118
1165
1044
1270
1155
Liquidus temp. (.degree.C.)
1125
1110
1110
1107
992 1107
1042
1112
1040
1230
1150
Chemical durability
2.2 4.3 3.4 3.3 6.9 3.3 10 0.8 4.2 3.8 5.2
Electrical resistance
11.4
11.7
11.3
11.5
12.4
11.5
11.6
11 8.8 8.4 10.9
__________________________________________________________________________
The glass composition of the present invention is scarcely brittle and has
a strain point of at least 560.degree. C. and a linear thermal expansion
coefficient close to that of soda lime glass, whereby it can be used for
an application where a high strain point is required among glass
substrates for which soda lime glass has heretofore been used. It is
particularly useful for a plasma display substrate, but it is also useful
for other substrates such as substrates for e.g. liquid crystal devices.
Further, the glass composition of the present invention has a high
electrical resistance of at least 10.sup.11 .OMEGA..multidot.cm at
150.degree. C., and it is accordingly useful for an application where
electrical insulation is particularly required.
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